Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution’s experience

AIM: The aim of this study was to identify the clinical and immunologic features of patients with 22q11.2 deletion syndrome who were followed up in our clinic. Thus, it is aimed to identify the syndrome early, choose the right treatment options according to humoral and cellular immunologic analysis,...

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Detalles Bibliográficos
Autores principales: Nepesov, Serdar, Aygün, Fatma Deniz, Küçüksezer, Umut, Taşdemir, Emre, Çokuğraş, Haluk, Camcıoğlu, Yıldız
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559977/
https://www.ncbi.nlm.nih.gov/pubmed/31217706
http://dx.doi.org/10.14744/TurkPediatriArs.2019.95815

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559977/
https://www.ncbi.nlm.nih.gov/pubmed/31217706
http://dx.doi.org/10.14744/TurkPediatriArs.2019.95815

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